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Please use this identifier to cite or link to this item: http://eprint.iitd.ac.in/handle/2074/155

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dc.contributor.authorBatheja, Raman-
dc.contributor.authorDhingra, S K-
dc.contributor.authorSingh, Ajai K-
dc.date.accessioned2005-04-29T11:21:46Z-
dc.date.available2005-04-29T11:21:46Z-
dc.date.issued1995-
dc.identifier.citationJournal of Organometallic Chemistry 496,99-102en
dc.identifier.urihttp://eprint.iitd.ac.in/dspace/handle/2074/155-
dc.description.abstractFive ternary complexes of palladium(II) namely [Pd(L1)2](C104)2 (1), [Pd(LIXL2)](C104)2 (2), [(PPh3)2Pd(LI)](C104)2 (3), [(DPPE)Pd(L2)](C104)2 (4) and [Pd(L1XL3)](C104)2 (5) where L 1 = MeSCH2CH2TeAr , L 2 = Me2NCH2CHzTeAr (At = 4-MeOC6H 4) and L 3 = MeSCH2CH(OH)CHzSMe were synthesized by treating [PdC12l1 (El)] or [(PPh3)z/(DPPE)PdCI2)] with AgC10 4 and the appropriate ligand. The ligands L a, L z and L 3 in these complexes are judged to be coordinated in bidentate mode on the basis of 1H NMR and IR spectral data. All the complexes behave as 1 : 2 electrolytes in CH3CN. The 125Te{1H} NMR spectra of 1 and 2 indicate that the ligands L 1 and L z in them are in a cis disposition in freshly prepared dimethylsulphoxide-d6-CD3CN solutions, implying a similar configuration in the solid state but within a few hours there is partial conversion into the trans isomer.en
dc.format.extent291056 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoen-
dc.subjectPalladiumen
dc.subjectTelluriumen
dc.subjectSulfuren
dc.titleTernary complexes of palladium(II) containing (Te,S) and (Te,N) hybrid organotellurium ligands: synthesis, spectra and cis-transisomeric conversionen
dc.typeArticleen
Appears in Collections:Chemistry

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